Question: Fastq Quality Trimmer For Pe Illumina?
0
gravatar for Kuehn, Joanna S [V MPM]
6.8 years ago by
Hello, I was wondering, can Galaxy's FASTQ Quality Trimmer tool be used on Illumina paired-end data? Would the forward and reverse read files need to be processed separately and be un-joinable afterwards for filtering? Thank you, Joanna
galaxy • 1.2k views
ADD COMMENTlink modified 6.8 years ago by Florent Angly370 • written 6.8 years ago by Kuehn, Joanna S [V MPM]10
0
gravatar for Florent Angly
6.8 years ago by
Florent Angly370
Florent Angly370 wrote:
Hi Joanna, During trimming, some of the reads may be removed from your dataset. Depending on what you need to do, you may or may not want to discard reads that don't have a "mate" mate anymore. If so, you might consider using the FASTQ de-interlacer and interlacer tools. Florent
ADD COMMENTlink written 6.8 years ago by Florent Angly370
Please log in to add an answer.

Help
Access

Use of this site constitutes acceptance of our User Agreement and Privacy Policy.
Powered by Biostar version 16.09
Traffic: 86 users visited in the last hour